Marcus R E, Catovsky D, Johnson S A, Gregory W M, Talavera J G, Goldman J M, Galton D A
Br J Cancer. 1986 Feb;53(2):175-80. doi: 10.1038/bjc.1986.32.
Between 1974 and 1984 69 adults with acute lymphoblastic leukaemia (ALL) were treated with two different protocols. Fifty-four (78%) of the patients entered complete remission (CR); 27 of these then received a consolidation protocol consisting of daunorubicin, cytosine arabinoside and 6-thioguanine, followed by two courses of intravenous methotrexate 500 mg m-2 with folinic acid rescue. All patients received intrathecal methotrexate and cranial irradiation (24 Gy) followed by maintenance therapy with 6-mercaptopurine and methotrexate for at least 2 years. The median survival for all patients was 23 months from the time of presentation with an actuarial 5-year survival of 21%. The actuarial chance of surviving 5 years in CR for patients receiving the consolidation protocol was 38% compared to 19% for patients receiving no consolidation (P = NS). Only patient age and white cell count at presentation were found to influence the chance of achieving CR and the chance of overall survival. The presence or absence of c-ALL antigen did not influence prognosis. Patients younger than 35 years with low white cell counts at presentation (less than 10 X 10(9)1(-1] had a particularly good prognosis but no patient with T-ALL and no patient older than 50 years old at diagnosis survived more than 18 months.
1974年至1984年间,69例成人急性淋巴细胞白血病(ALL)患者接受了两种不同的治疗方案。其中54例(78%)患者进入完全缓解(CR)状态;这54例患者中的27例随后接受了由柔红霉素、阿糖胞苷和6-硫鸟嘌呤组成的巩固治疗方案,之后是两个疗程的静脉注射甲氨蝶呤500 mg/m²并进行亚叶酸钙解救。所有患者均接受鞘内注射甲氨蝶呤和颅脑照射(24 Gy),随后用6-巯基嘌呤和甲氨蝶呤进行维持治疗至少2年。所有患者从确诊时起的中位生存期为23个月,5年预期生存率为21%。接受巩固治疗方案的患者在CR状态下存活5年的预期概率为38%,而未接受巩固治疗的患者为19%(P = 无显著差异)。仅发现确诊时的患者年龄和白细胞计数会影响达到CR的概率和总体生存概率。c-ALL抗原的有无不影响预后。确诊时年龄小于35岁且白细胞计数低(小于10×10⁹/L)的患者预后特别好,但T-ALL患者以及确诊时年龄大于50岁的患者均无存活超过18个月的。